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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorLo Prinzi, Federica
dc.contributor.authorsalani, francesca
dc.contributor.authorrimini, margherita
dc.contributor.authorRizzato, Mario Domenico
dc.contributor.authorAntonuzzo, Lorenzo
dc.contributor.authorCamera, Silvia
dc.contributor.authorCastet, Florian
dc.date.accessioned2025-04-09T08:38:53Z
dc.date.available2025-04-09T08:38:53Z
dc.date.issued2025-03
dc.identifier.citationLo Prinzi F, Salani F, Rimini M, Rizzato MD, Antonuzzo L, Camera S, et al. Efficacy of cisplatin-gemcitabine-durvalumab in patients with advanced biliary tract cancer experiencing early vs late disease relapse after surgery: a large real-life worldwide population. Oncologist. 2025 Mar;30(3):oyae256.
dc.identifier.issn1549-490X
dc.identifier.urihttp://hdl.handle.net/11351/12921
dc.descriptionAdvanced disease; Biliary tract cancer; Surgery
dc.description.abstractBackground: In the TOPAZ-1, patients with biliary tract cancers (BTC) and recurrence within 6 months after surgery were excluded, even if this event is frequently observed in clinical practice. Our study aimed to assess if the efficacy of cisplatin-gemcitabine-durvalumab (CGD) in this population is comparable to that reported in the phase 3 trial. Methods: The study cohort included patients with BTC who underwent surgery on the primary tumor, experienced disease recurrence occurring ≤6 months or >6 months after surgery or after the end of adjuvant therapy and started CGD. The primary objectives were overall survival (OS) and progression free survival (PFS). Results: A total of 178 patients were enrolled. No significant differences were observed between early and late relapse groups in OS (23.4 months vs not reached; HR 1.26; 95% CI, 0.67-2.37; P = .45) and PFS [7.0 months vs 9.8 months; HR 1.3(95% CI, 0.9-2.1) P = .13]. Overall response rate and disease control rate (P = .33 and P = .62) were comparable between the 2 groups, as the overall safety profile. In addition, we compared survival outcomes between the selected population and a historical cohort of patients with BTC treated with cisplatin-gemcitabine (CG) and found that despite the absence of statistical significance, CGD showed an outcome trend compared with CG regardless of the time of recurrence after surgery or adjuvant chemotherapy [(CG ≤ 6 vs CGD ≤ 6 months: HR 0.59, 95%CI, 0.35-1.01, P = .05; HR 0.70; 95%CI, 0.46-1.06, P = .09, OS and PFS, respectively) and (CG > 6 vs. CGD > 6 months: HR 0.50; 95%CI, 0.29-0.88, P = 0.0165; HR 0.54; 95%CI, 0.35-0.84, P = .0068, OS and PFS, respectively)]. Conclusion: Our analysis suggests that CGD retains its efficacy independently of the timing of relapse after surgery or completion of adjuvant treatment in patients with advanced BTC.
dc.language.isoeng
dc.publisherOxford University Press
dc.relation.ispartofseriesThe Oncologist;30(3)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectQuimioteràpia combinada
dc.subjectTracte biliar - Càncer - Tractament
dc.subjectTracte biliar - Càncer - Cirurgia
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshBiliary Tract Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshBiliary Tract Neoplasms
dc.subject.mesh/surgery
dc.titleEfficacy of cisplatin-gemcitabine-durvalumab in patients with advanced biliary tract cancer experiencing early vs late disease relapse after surgery: a large real-life worldwide population
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1093/oncolo/oyae256
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada
dc.subject.decsneoplasias del tracto biliar
dc.subject.decs/farmacoterapia
dc.subject.decsneoplasias del tracto biliar
dc.subject.decs/cirugía
dc.relation.publishversionhttps://doi.org/10.1093/oncolo/oyae256
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Lo Prinzi F] Operative Research Unit of Medical Oncology, Fondazione Policlinico Universitario Campus Bio-Medico, Roma, Italy. [Salani F] Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy. Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy. [Rimini M] Department of Oncology, Vita-Salute San Raffaele University, IRCCS San Raffaele Scientifc Institute Hospital, Milan, Italy. [Rizzato MD] Department of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy. [Antonuzzo L] Clinical Oncology Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, University of Florence, Florence, Italy. Thoracic Surgery Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, University of Florence, Florence, Italy. [Camera S] Department of Oncology, Vita-Salute San Raffaele University, IRCCS San Raffaele Scientifc Institute Hospital, Milan, Italy. [Castet F] Gastrointestinal and Endocrine Tumor Unit, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid39427227
dc.identifier.wos001339164500001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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